Assessment of Needs of Moisturizers After Various Laser Treatments

March 29, 2016 updated by: Pusan National University Hospital

Phase 4 Study of Assessment of Needs of Moisturizers After Various Laser Treatment

Assessment of needs of moisturizers after various laser treatments

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

The investigators would like to assess of needs of moisturizers after various laser treatment

: by investigating the changes in the skin barrier function after fractional carbon dioxide laser and fractional Er:Glass laser in mice and human skin

Study Type

Interventional

Enrollment (Actual)

20

Phase

  • Phase 4

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Korea, Republic of
      • Busan, Korea, Republic of
        • Department of dermatology, Pusan National University Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 60 years (Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • at least 18 years of age without any dermatologic diseases

Exclusion Criteria:

  • Taking other known dermatologic disease
  • Others who are shown pigmented lesion on treated-area
  • Who have allergy or history of hypersensitivity reaction to moisturizers
  • Who have other definitive cutaneous findings

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Physiogel, Laser therapy, Moisturizer

Experimental: Physiogel treated & Non-treated

1 Palmitoylethanolamide, Physiogel 3 times a day for 2 weeks
Other: Physiogel
Application of moisturizer on laser-treated area
Other Names:
  • Other moisturizer: Palmitoylethanolamide
  • Other Names:Physiogel
Other: Moisturizer
Application of moisturizer on laser-treated area
Other Names:
  • Other moisturizer: Palmitoylethanolamide
  • Other Names:Physiogel

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Clinical assessment of erythema, transepidermal water loss
Time Frame: 2weeks
The clinical assessment of erythema, pigmentation, transepidermal water loss will be evaluated by using apparatus.
2weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Pusan National University Hospital

Investigators

  • Study Chair: Byung-Soo Kim, Ph.D., Pusna National University Hospital

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

September 1, 2012

Primary Completion (Actual)

April 1, 2015

Study Completion (Actual)

December 1, 2015

Study Registration Dates

First Submitted

December 3, 2012

First Submitted That Met QC Criteria

December 4, 2012

First Posted (Estimate)

December 5, 2012

Study Record Updates

Last Update Posted (Estimate)

March 30, 2016

Last Update Submitted That Met QC Criteria

March 29, 2016

Last Verified

March 1, 2016

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • PNUHDM-laser and moisturizers

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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